Foessleitner Philipp, Gasser Julia, Kiss Herbert, Flunt Albert, Presterl Elisabeth, Petricevic Ljubomir, Farr Alex
Department of Obstetrics and Gynecology, Division of Obstetrics and Feto-Maternal Medicine, Medical University of Vienna, Vienna, Austria.
Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.
Eur J Obstet Gynecol Reprod Biol. 2020 Mar;246:86-89. doi: 10.1016/j.ejogrb.2020.01.025. Epub 2020 Jan 21.
Extended-spectrum beta-lactamase (ESBL) is a rapidly evolving enzyme that cleaves beta-lactam-containing antibiotics, forming resistance to certain types of antibiotics, such as penicillin, cephalosporins and monobactams. Colonization with ESBL-producing bacteria during pregnancy is harmful, however this topic is currently underrepresented in the literature.
Using a retrospective design, we analyzed data of all consecutive pregnant women who were identified with a vaginal colonization of ESBL-producing bacteria from 2011 to 2016 at the Medical University of Vienna, Department of Obstetrics and Gynecology. Swabs were taken during pregnancy and/or at delivery, as well as from neonates. Demographic and clinical data were obtained from the central in-house alert system and patients' clinical records.
Of the 14,279 deliveries performed in our department during the study period, we identified 13 women with vaginal colonization of ESBL-producing bacteria during pregnancy. Of these cases, 6 born neonates were tested ESBL positive. The maternal-to-neonatal transmission rate was 43 %, associated with a 70 % rate of preterm premature rupture of the membranes (pPROM) and a preterm birth rate of 83 %. Of the 6 neonates with ESBL colonization, 4 neonates (67 %) were born to mothers who were still tested positive at the time of delivery.
Maternal colonization of ESBL-producing bacteria is an important risk factor for transmission. The vaginal presence of ESBL-producing bacteria during pregnancy is associated with preterm birth and pPROM, which shows the need for clear diagnostic and therapeutic guidelines.
超广谱β-内酰胺酶(ESBL)是一种快速演变的酶,可裂解含β-内酰胺的抗生素,从而对某些类型的抗生素产生耐药性,如青霉素、头孢菌素和单环β-内酰胺类抗生素。孕期产ESBL细菌的定植是有害的,然而该主题目前在文献中报道较少。
采用回顾性设计,我们分析了2011年至2016年在维也纳医科大学妇产科确诊为产ESBL细菌阴道定植的所有连续孕妇的数据。在孕期和/或分娩时以及从新生儿处采集拭子。人口统计学和临床数据从中央内部警报系统和患者临床记录中获取。
在研究期间我们科室进行的14279例分娩中,我们确定了13例孕期产ESBL细菌阴道定植的女性。在这些病例中,6例出生的新生儿ESBL检测呈阳性。母婴传播率为43%,与70%的胎膜早破早产(pPROM)率和83%的早产率相关。在6例有ESBL定植的新生儿中,4例(67%)的母亲在分娩时仍检测呈阳性。
产ESBL细菌的母体定植是传播的重要危险因素。孕期阴道存在产ESBL细菌与早产和pPROM相关,这表明需要明确的诊断和治疗指南。